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JIMD Reports
|
February 23, 2013
Onset of adreno-leukodystrophy after medulloblastoma therapy: causal connection or coincidence?
G Deib, A Poretti, A Meoded, et al.
American Journal of Medical Genetics. Part A
|
April 6, 2005
A novel MGP mutation in a consanguineous family: review of the clinical and molecular characteristics of Keutel syndrome
David J Hur, Gerald V Raymond, Stephen G Kahler, et al.
Cancer Treatment Reports
|
June 1, 1987
Phase II trial of idarubicin in patients with pancreatic cancer
A Mittelman, G B Magill, V Raymond, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
April 5, 2022
Nervonic Acid Attenuates Accumulation of Very Long-Chain Fatty Acids and is a Potential Therapy for Adrenoleukodystrophy
Marcia R Terluk, Julianne Tieu, Siddhee A Sahasrabudhe, et al.
Neuropediatrics
|
February 24, 2001
X-Linked adrenoleukodystrophy: overview and prognosis as a function of age and brain magnetic resonance imaging abnormality. A study involving 372 patients
H W Moser, D J Loes, E R Melhem, et al.
Journal of Biopharmaceutical Statistics
|
August 23, 2016
A hierarchical Bayesian approach for combining pharmacokinetic/pharmacodynamic modeling and Phase IIa trial design in orphan drugs: Treating adrenoleukodystrophy with Lorenzo's oil
Cynthia Basu, Mariam A Ahmed, Reena V Kartha, et al.
Plos One
|
November 28, 2012
Cerebrospinal fluid matrix metalloproteinases are elevated in cerebral adrenoleukodystrophy and correlate with MRI severity and neurologic dysfunction
Kathryn A Thibert, Gerald V Raymond, David R Nascene, et al.
Scientific Reports
|
December 3, 2016
Elevated cerebral spinal fluid biomarkers in children with mucopolysaccharidosis I-H
Gerald V Raymond, Marzia Pasquali, Lynda E Polgreen, et al.
American Journal of Human Genetics
|
June 1, 1995
A common gene for juvenile and adult-onset primary open-angle glaucomas confined on chromosome 1q
J Morissette, G Côté, J L Anctil, et al.
Annals of Neurology
|
September 1, 1995
Distinction between peroxisomal bifunctional enzyme and acyl-CoA oxidase deficiencies
P A Watkins, M C McGuinness, G V Raymond, et al.
Page
of 22
Search research articles
Search
Showing results (101-110 of 214) with videos related to
Sort By:
Page
of 22
JIMD Reports
|
February 23, 2013
Onset of adreno-leukodystrophy after medulloblastoma therapy: causal connection or coincidence?
G Deib, A Poretti, A Meoded, et al.
American Journal of Medical Genetics. Part A
|
April 6, 2005
A novel MGP mutation in a consanguineous family: review of the clinical and molecular characteristics of Keutel syndrome
David J Hur, Gerald V Raymond, Stephen G Kahler, et al.
Cancer Treatment Reports
|
June 1, 1987
Phase II trial of idarubicin in patients with pancreatic cancer
A Mittelman, G B Magill, V Raymond, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
April 5, 2022
Nervonic Acid Attenuates Accumulation of Very Long-Chain Fatty Acids and is a Potential Therapy for Adrenoleukodystrophy
Marcia R Terluk, Julianne Tieu, Siddhee A Sahasrabudhe, et al.
Neuropediatrics
|
February 24, 2001
X-Linked adrenoleukodystrophy: overview and prognosis as a function of age and brain magnetic resonance imaging abnormality. A study involving 372 patients
H W Moser, D J Loes, E R Melhem, et al.
Journal of Biopharmaceutical Statistics
|
August 23, 2016
A hierarchical Bayesian approach for combining pharmacokinetic/pharmacodynamic modeling and Phase IIa trial design in orphan drugs: Treating adrenoleukodystrophy with Lorenzo's oil
Cynthia Basu, Mariam A Ahmed, Reena V Kartha, et al.
Plos One
|
November 28, 2012
Cerebrospinal fluid matrix metalloproteinases are elevated in cerebral adrenoleukodystrophy and correlate with MRI severity and neurologic dysfunction
Kathryn A Thibert, Gerald V Raymond, David R Nascene, et al.
Scientific Reports
|
December 3, 2016
Elevated cerebral spinal fluid biomarkers in children with mucopolysaccharidosis I-H
Gerald V Raymond, Marzia Pasquali, Lynda E Polgreen, et al.
American Journal of Human Genetics
|
June 1, 1995
A common gene for juvenile and adult-onset primary open-angle glaucomas confined on chromosome 1q
J Morissette, G Côté, J L Anctil, et al.
Annals of Neurology
|
September 1, 1995
Distinction between peroxisomal bifunctional enzyme and acyl-CoA oxidase deficiencies
P A Watkins, M C McGuinness, G V Raymond, et al.
Page
of 22